Coping With Myasthenia GravisThis section is a place to share stories about Coping With Myasthenia Gravis Below are entries of those who have already shared their stories. We hope that you find their experiences helpful to your own situation. You may also Help others by sharing your story. To quickly access health information from your website's browser, download MG - I was just very recently diagnosed I can share Sharon’s story about the couch and not being able to do the things that I have always done. I kept telling everyone something was wrong and I was so tired and extremly weak, all the time. No appetite, nausea and what goes in must come out. My children are 27 and 18, my 18 year old I barely made it to his Graduation, but I would not have missed that for anything. I did buy him a new Eclipse, manly hunter green for graduation, but that took every bit of energy I had, but sometimes (this was before I was diagnosed) I would have to plan things 3-5 days in advance. I was just diagnosed August 15, 2008. Now they are going for my Thymus gland on Monday, Sept 1, 2008. The CRT scans have been horrible, the 1st one blew a vein and I ended up in ER two times w/t 2 days, not fun. My Dr. has started me on losts of anti-biotics for ulcers and ulcerative coalitice. God Bless Comments
September 2008
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